JPH0343784B2 - - Google Patents
Info
- Publication number
- JPH0343784B2 JPH0343784B2 JP57046611A JP4661182A JPH0343784B2 JP H0343784 B2 JPH0343784 B2 JP H0343784B2 JP 57046611 A JP57046611 A JP 57046611A JP 4661182 A JP4661182 A JP 4661182A JP H0343784 B2 JPH0343784 B2 JP H0343784B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- less
- particle size
- silica powder
- powder
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10W—GENERIC PACKAGES, INTERCONNECTIONS, CONNECTORS OR OTHER CONSTRUCTIONAL DETAILS OF DEVICES COVERED BY CLASS H10
- H10W74/00—Encapsulations, e.g. protective coatings
- H10W74/40—Encapsulations, e.g. protective coatings characterised by their materials
- H10W74/47—Encapsulations, e.g. protective coatings characterised by their materials comprising organic materials, e.g. plastics or resins
- H10W74/473—Encapsulations, e.g. protective coatings characterised by their materials comprising organic materials, e.g. plastics or resins containing a filler
Landscapes
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
この発明は成形時の流動性が良好でかつバリの
出方が少なく、しかも金型摩耗の少ない半導体封
止用樹脂組成物に関する。
近年、半導体素子の封止は、量産性、経済性に
すぐれているトランスフアー成形が主流になつて
いるが、適用素子の拡大や高信頼性への追求とと
もに、成形樹脂への要求特性も一段と厳しくなつ
ている。とくに、ICの集積度の向上とともにチ
ツプサイズの拡大とパワーアツプに対する樹脂の
改良が望まれている。
このような要求特性にこたえる封止材料のひと
つとして、熱膨脹率の小さい溶融性シリカと熱伝
導性の高い結晶性シリカとを充填剤として併用し
た、つまりエポキシ樹脂などに上記両シリカを共
に含ませてなるものが知られている。この種の封
止材料によれば、チツプに対する熱的歪が小さく
なつてチツプクラツクや樹脂クラツクが抑えら
れ、しかもチツプから発生する熱が効率よく外部
に放散されてチツプの温度上昇が抑えられるた
め、半導体の信頼性を大きく向上させることがで
きる。
ところが、かかる混合シリカを用いた封止材料
にあつては、成形時の流動性が充分でなかつた
り、逆に流動しすぎてバリが発生しやすくなつた
り、また金型の摩耗が著るしくなる場合があるな
ど、成形作業性の面で必らずしも満足できるもの
とはいえなかつた。
この発明者らは、上記の原因につき鋭意検討を
重ねたた結果、上述の如き問題が主として使用す
る溶融性シリカ粉末と結晶性シリカ粉末の粒子径
に起因するものであることを知り、この粒子径を
特定範囲に設定してかつ両シリカの混合比率およ
び組成物全体に占める混合シリカの含有量を特定
することにより、流動性、バリおよび金型摩耗の
面でいずれも好結果が得られることを知り、この
発明を完成するに至つたものである。
すなわち、この発明は、(A)粒度が46μ以上30重
量%以上、149μ以上1重量%以下の溶融性シリ
カ粉末と、(B)粒度が46μ以上1重量%以下、10μ
以下60重量%以上の結晶性シリカ粉末とからな
り、かつA/(A+B)が0.3〜0.7である充填剤
粉末を60〜85重量%含むことを特徴とする半導体
封止用樹脂組成物に係るものである。
この発明において用いる上記ふたつのシリカ粉
末の粒子径につき詳述すると、まず、粒度が46μ
以上30重量%以上の溶融性シリカ粉末を使用する
一方粒度が46μ以上1重量%以下の結晶性シリカ
粉末を使用することによつて、つまりは粒度の粗
いものとして溶融性シリカ粉末を用いることによ
り、金型摩耗を減少できる効果が得られる。ま
た、粒子径の小さくされた上記結晶性シリカ粉末
は、これが10μ以下60重量%以上とされているこ
とによつて、混合粉末全体の粒子径のバンス特性
に好結果を与えて、流動性とバリ特性とを共に満
足させる。さらに、溶融性シリカの粒度が149μ
以上1重量%以下とされていることにより、成形
時のゲートつまりが防止される。
この発明において、A/(A+B)、つまり溶
融性シリカ粉末と結晶性シリカ粉末との合計量に
対する溶融性シリカの比率を0.3〜0.7に設定した
のは、この範囲によつてのみ流動性とバリ特性と
を共に満足させることができるからである。すな
わち、上記比率が0.3に満たないときは、流動性
が低下し、逆に上記比率が0.7より大きくなると
バリが発生しやすい。
溶融性シリカ粉末と結晶性シリカ粉末とからな
る混合シリカの組成物全体に占める割合は、60〜
85重量%とすべきであり、60重量%より少ないと
熱膨脹係数が大きくなりすぎたり熱伝導性が悪く
なるし、また85重量%より多くなると流動性が極
端に悪くなつたり、キヤビテイーへの樹脂の回り
込みが悪くなつて成形性が損なわれる。
この発明において使用する上記両シリカは、高
純度である必要があり、例えばシリカ1gに対し
純水10gで煮沸した際の抽出液の電気伝導度が
10μν/cm以下、Naが5ppm以下、clが5ppm以下
のものが望ましい。
この発明において用いられる樹脂分としては、
熱硬化性樹脂であれば広く包含されるが、特にエ
ポキシ樹脂、例えばフエノールノボラツク型エポ
キシ樹脂、クレゾールノボラツク型エポキシ樹
脂、ビスフエノールA型エポキシ樹脂、脂環型エ
ポキシ樹脂が好適である。また、硬化剤は公知の
もの、例えばフエノール樹脂、アミン、酸無水
物、イソシアネートなど、特に制限なく使用が可
能である。
この発明の半導体封止用樹脂組成物には、この
発明の目的の範囲内で、他の添加剤例えば着色
剤、難燃剤、離型剤、カツプリング剤、硬化促進
剤などを配合することができる。特に、硬化性を
早めるため、硬化促進剤として、イミダゾール
類、イミダゾリン類、3級アミンなどの単独ある
いは2種以上を配合することが好ましい。
この発明の半導体封止用樹脂組成物の調製に当
たつての混練もしくは混合は、加熱ロールによる
溶融混練、釜による溶融混練、押出機による溶融
混練など、またそれらの組合せを適宜選択でき
る。
次に、この発明の実施例を記載する。
実施例
エポキシ当量220、軟化点75℃のクレゾールノ
ボラツクエポキシ樹脂16部、エポキシ当量275、
軟化点79℃の難燃化エポキシ樹脂2.5部、水酸基
当量105、軟化点76℃のフエノールノボラツク樹
脂8.0部、2−メチルイミダゾール0.4部、カルナ
バワツクス0.3部、シランカツプリング剤0.5部、
三酸化アンチモン1.8部およびカーボンブツク0.3
部のほかに、第1表に示すような粒度を持つシリ
カ粉末を第2表に示す組成比(重量部)で使用
し、つぎの如き手法にて、比較例を含め8種の半
導体封止用樹脂組成物を製造した。
ななわち、まず、充填剤および三酸化アンチモ
ンをカツプリング剤で混合処理し、その後残余の
材料を加え、さらに粉砕混合し、次に80℃に加熱
したミキシングロールにて10分間混練した後シー
ト状にした。これを冷却粉砕して半導体封止用樹
脂組成物粉末を得た。
The present invention relates to a resin composition for semiconductor encapsulation that has good fluidity during molding, has less burrs, and has less mold wear. In recent years, transfer molding has become the mainstream for encapsulating semiconductor devices due to its excellent mass production and economic efficiency.However, with the expansion of applicable devices and the pursuit of high reliability, the characteristics required for molding resins have also become more important. It's getting tougher. In particular, it is desired to improve the degree of integration of ICs, increase the chip size, and improve resins for power-up. One type of sealing material that meets these required characteristics is one that uses both fused silica, which has a low coefficient of thermal expansion, and crystalline silica, which has high thermal conductivity, as fillers, that is, contains both of the above silicas in an epoxy resin, etc. It is known that This type of sealing material reduces thermal strain on the chip, suppressing chip cracks and resin cracks, and also efficiently dissipates heat generated from the chip to the outside, suppressing the temperature rise of the chip. The reliability of semiconductors can be greatly improved. However, in the case of sealing materials using such mixed silica, fluidity during molding may not be sufficient, or on the contrary, it may flow too much, making it easy for burrs to occur, and mold wear may be significant. In some cases, the process was not always satisfactory in terms of molding workability. As a result of intensive investigation into the causes of the above, the inventors found that the above-mentioned problems were mainly caused by the particle sizes of the fusible silica powder and crystalline silica powder used, and found that the particles By setting the diameter within a specific range and specifying the mixing ratio of both silicas and the content of mixed silica in the entire composition, good results can be obtained in terms of fluidity, burrs, and mold wear. This led to the completion of this invention. That is, this invention provides (A) fusible silica powder with a particle size of 46μ or more and 30% by weight or more, 149μ or more and 1% by weight or less, and (B) a fusible silica powder with a particle size of 46μ or more and 1% by weight or less, and 10μ
A resin composition for semiconductor encapsulation characterized by comprising 60% by weight or more of crystalline silica powder and 60 to 85% by weight of filler powder having an A/(A+B) of 0.3 to 0.7. It is something. To explain in detail the particle size of the two silica powders used in this invention, first, the particle size is 46 μm.
By using fusible silica powder with a particle size of 30% or more and by using crystalline silica powder with a particle size of 46μ or more and 1% by weight or less, that is, by using fusible silica powder with a coarse particle size. , the effect of reducing mold wear can be obtained. In addition, the above-mentioned crystalline silica powder with a reduced particle size has a particle size of 10μ or less and 60% by weight or more, which gives good results to the bounce characteristics of the particle size of the entire mixed powder and improves fluidity. Both the burr characteristics and the burr characteristics are satisfied. In addition, the particle size of fusible silica is 149μ
By setting the content to 1% by weight or less, clogging of the gate during molding can be prevented. In this invention, A/(A+B), that is, the ratio of fusible silica to the total amount of fusible silica powder and crystalline silica powder, is set to 0.3 to 0.7. This is because both characteristics can be satisfied. That is, when the above ratio is less than 0.3, fluidity decreases, and conversely, when the above ratio is greater than 0.7, burrs are likely to occur. The proportion of mixed silica consisting of fusible silica powder and crystalline silica powder in the entire composition is 60 to 60%.
It should be 85% by weight; if it is less than 60% by weight, the coefficient of thermal expansion will be too large and the thermal conductivity will be poor, and if it is more than 85% by weight, the fluidity will be extremely poor or the resin will not enter the cavity. The wraparound becomes poor and moldability is impaired. The above-mentioned silicas used in this invention need to be of high purity. For example, when 1 g of silica is boiled with 10 g of pure water, the electrical conductivity of the extract is
Desirably, the content is 10μν/cm or less, Na is 5ppm or less, and Cl is 5ppm or less. The resin content used in this invention is as follows:
Although a wide variety of thermosetting resins are included, epoxy resins such as phenol novolac type epoxy resins, cresol novolak type epoxy resins, bisphenol A type epoxy resins, and alicyclic type epoxy resins are particularly suitable. Furthermore, known curing agents such as phenolic resins, amines, acid anhydrides, and isocyanates can be used without particular limitation. The resin composition for semiconductor encapsulation of the present invention may contain other additives such as colorants, flame retardants, mold release agents, coupling agents, curing accelerators, etc. within the scope of the purpose of the present invention. . In particular, in order to speed up the curing properties, it is preferable to mix one or more of imidazoles, imidazolines, tertiary amines, etc. as curing accelerators. The kneading or mixing in preparing the resin composition for semiconductor encapsulation of the present invention may be performed by melt-kneading using heated rolls, melt-kneading using a pot, melt-kneading using an extruder, or any combination thereof. Next, examples of this invention will be described. Example Epoxy equivalent: 220, 16 parts of cresol novolak epoxy resin with a softening point of 75°C, epoxy equivalent: 275,
2.5 parts of flame-retardant epoxy resin with a softening point of 79°C, hydroxyl equivalent 105, 8.0 parts of phenol novolac resin with a softening point of 76°C, 0.4 parts of 2-methylimidazole, 0.3 parts of carnauba wax, 0.5 parts of silane coupling agent,
1.8 parts of antimony trioxide and 0.3 parts of carbon book
In addition, silica powder having the particle size shown in Table 1 was used in the composition ratio (parts by weight) shown in Table 2, and 8 types of semiconductor encapsulation including comparative examples were performed using the following method. A resin composition for use was produced. That is, first, the filler and antimony trioxide are mixed with a coupling agent, then the remaining materials are added, further pulverized and mixed, and then kneaded for 10 minutes with a mixing roll heated to 80°C, and then shaped into a sheet. I made it. This was cooled and pulverized to obtain a resin composition powder for semiconductor encapsulation.
【表】
得られた樹脂組成物粉末につき、流動性の指
針としてEMMI−I−66に準じてスパイラルフ
ローを測定した。バリの出方を調べるため、
5μの隙間を設けた金型でトランスフアー成形
(175℃、5分)し、隙間から出るバリの長さを評
価した。金型の摩耗性を調べるため、焼き入れ
しない型を用い成形した後のゲート部の摩耗度を
評価した。これらの結果はつぎの第2表に示され
るとおりであつた。[Table] The spiral flow of the obtained resin composition powder was measured according to EMMI-I-66 as a guideline for fluidity. To find out how burrs appear,
Transfer molding was performed (175°C, 5 minutes) using a mold with a 5μ gap, and the length of burrs coming out of the gap was evaluated. In order to investigate the abrasion resistance of the mold, the degree of wear of the gate portion after molding using a non-quenched mold was evaluated. These results were as shown in Table 2 below.
【表】
上記の結果から明らかなように、この発明の半
導体封止用樹脂組成物は、流動性とバリ特性とを
共に満足してしかも金型摩耗性も少ないというす
ぐれた特徴を有しており、溶融性シリカと結晶性
シリカとの併用による熱膨脹率および熱伝導性の
本来の特性を活かしうる工業的有用な樹脂組成物
を提供できるものであることがわかる。[Table] As is clear from the above results, the resin composition for semiconductor encapsulation of the present invention has excellent characteristics in that it satisfies both fluidity and burr properties and has low mold abrasion. This shows that it is possible to provide an industrially useful resin composition that can take advantage of the inherent characteristics of thermal expansion coefficient and thermal conductivity due to the combined use of fused silica and crystalline silica.
Claims (1)
1重量%以下の溶融性シリカ粉末と、 (B) 粒度が46μ以上1重量%以下、10μ以下60重
量%以上の結晶性シリカ粉末とからなり、かつ
A/(A+B)が0.3〜0.7である充填剤粉末を
60〜85重量%含むことを特徴とする半導体封止
用樹脂組成物。[Scope of Claims] 1 (A) Fusible silica powder with a particle size of 46μ or more and 30% by weight or more, 149μ or more and 1% by weight or less, and (B) a particle size of 46μ or more and 1% by weight or less and 10μ or less and 60% by weight or more filler powder consisting of crystalline silica powder and having A/(A+B) of 0.3 to 0.7.
A resin composition for semiconductor encapsulation characterized by containing 60 to 85% by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57046611A JPS58164250A (en) | 1982-03-24 | 1982-03-24 | Resin composition for sealing semiconductor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57046611A JPS58164250A (en) | 1982-03-24 | 1982-03-24 | Resin composition for sealing semiconductor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58164250A JPS58164250A (en) | 1983-09-29 |
| JPH0343784B2 true JPH0343784B2 (en) | 1991-07-03 |
Family
ID=12752093
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57046611A Granted JPS58164250A (en) | 1982-03-24 | 1982-03-24 | Resin composition for sealing semiconductor |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58164250A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6181422A (en) * | 1984-09-28 | 1986-04-25 | Toshiba Corp | Epoxy resin composition for casting |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5610947A (en) * | 1979-07-10 | 1981-02-03 | Toshiba Corp | Semiconductor sealing resin composition |
-
1982
- 1982-03-24 JP JP57046611A patent/JPS58164250A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58164250A (en) | 1983-09-29 |
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